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CMD
Congenital muscular dystrophy
Congenital muscular dystrophy NOS
Congenital muscular dystrophy type 1B
Congenital muscular dystrophy with hyperlaxity
Disease central core
FCMD
Fukuyama-type congenital muscular dystrophy
Minicore
Multicore
Nemaline
Salih congenital muscular dystrophy

Translation of "Salih congenital muscular dystrophy " (English → French) :

Salih congenital muscular dystrophy

myopathie précoce avec cardiomyopathie létale
SNOMEDCT-BE (disorder) / 702343002
SNOMEDCT-BE (disorder) / 702343002


Fukuyama-type congenital muscular dystrophy | FCMD [Abbr.]

dystrophie musculaire congénitale de Fukuyama
IATE - Health
IATE - Health


congenital muscular dystrophy | CMD [Abbr.]

dystrophie musculaire congénitale | DMC [Abbr.]
IATE - Health
IATE - Health


Congenital muscular dystrophy type 1B

dystrophie musculaire congénitale type 1B
SNOMEDCT-BE (disorder) / 764944006
SNOMEDCT-BE (disorder) / 764944006


Congenital muscular dystrophy with hyperlaxity

dystrophie musculaire congénitale avec hyperlaxité
SNOMEDCT-BE (disorder) / 763314009
SNOMEDCT-BE (disorder) / 763314009


Congenital muscular dystrophy:NOS | with specific morphological abnormalities of the muscle fibre | Disease:central core | minicore | multicore | Fibre-type disproportion Myopathy:myotubular (centronuclear) | nemaline

Disproportion des types de fibres Dystrophie musculaire congénitale:SAI | avec anomalies morphologiques spécifiques des fibres musculaires | Myopathie:à axe central | à bâtonnets [némaline] | de type: mini-core | multi-core | myotubulaire (centro-nucléaire)
WORLD HEALTH ORGANIZATION ICD-10: G71.2
WORLD HEALTH ORGANIZATION ICD-10: G71.2




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'Salih congenital muscular dystrophy'

Date index:2022-08-28 -

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